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Incentives for Participation Versus Outcomes

U

University of Rhode Island

Status

Withdrawn

Conditions

Smoking

Treatments

Behavioral: Incentives for Participation
Behavioral: Incentives for Cessation

Study type

Interventional

Funder types

Other

Identifiers

NCT01826331
DA034041

Details and patient eligibility

About

One of the most important debates in the field of disease prevention is whether financial incentives should be contingent on participation in evidence-based programs for smoking cessation or on actual outcomes, like prolonged abstinence. This study can fill a major knowledge gap in this debate, which is the lack of any population trial that compared the impacts of outcomes- and participation-based incentives in a population of smokers. This research can help policy makers and health service providers choose the incentives approach that provides the most effectiveness, cost-effectiveness and cost-savings for entire populations of smokers.

Full description

This population-based randomized clinical trial is designed to compare long-term abstinence rates in three groups of smokers: 1. Those incentivized for participation in an evidence-based treatment designed for smokers at each stage of change; 2. Those incentivized for biologically validated prolonged abstinence at 6 and 12 months who could also choose to participate in the TTM (Transtheoretical Model)-tailored intervention; and 3. An assessment only control condition.

The Specific Aims are:

  1. To assess whether the treatment group incentivized for participation outperforms the control group at 12, 24 and 36 months as hypothesized;
  2. To assess whether the treatment group incentivized for prolonged abstinence at 6 and 12 months outperforms the control group at each follow-up as hypothesized;
  3. To assess whether the treatment group incentivized for participation outperforms the treatment group incentivized for outcomes at 36 months as hypothesized.
  4. To compare the cost-effectiveness of each treatment in a population of mostly unmotivated smokers;

The Secondary Aims are:

  1. To assess the long-term treatment trajectories of each treatment compared to controls with hypothesized increasing trajectory in the participation contingent incentives and decreasing trajectory in the outcome contingent incentives.
  2. To identify mediators of long-term outcomes in each treatment, such as amount of treatment participation, income, severity of smoking, stage of change, self-efficacy, perceived health and intrinsic and extrinsic motivation to quit.
  3. To compare cost-savings of each treatment by modeling all additional costs of smoking for employers and smokers.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • smoker

Exclusion criteria

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Single Blind

0 participants in 3 patient groups

Control Group
No Intervention group
Description:
Participants will be incentivized for assessments only
Incentives for Participation
Experimental group
Description:
Participants will be incentivized for each assessment and for each smoking cessation session they complete
Treatment:
Behavioral: Incentives for Participation
Incentives for Cessation
Experimental group
Description:
Participants will be incentivized for each assessment and biochemically confirmed abstinence at 12 and 24 months
Treatment:
Behavioral: Incentives for Cessation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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